Until recently, little was known about the fungi found in shark gills and their biomedicinal potential. In this article, we described the isolation, bioactivity, diversity, and secondary metabolites of bioactive fungi...Until recently, little was known about the fungi found in shark gills and their biomedicinal potential. In this article, we described the isolation, bioactivity, diversity, and secondary metabolites of bioactive fungi from the gill of a shark （Carcharodon carcharias）. A total of 115 isolates were obtained and grown in 12 culture media. Fifty-eight of these isolates demonstrated significant activity in four antimicrobial, pesticidal, and cytotoxic bioassay models. Four randomly selected bioactive isolates inhibited human cancer cell proliferation during re-screening. These active isolates were segregated into 6 genera using the internal transcribed spacer-large subunit （ITS-LSU） rDNA-sequence BLAST comparison. Four genera, Penicillium, Aspergillus, Mucor, and Chaetomium were the dominant taxa. A phylogenic tree illustrated their intergenera and intragenera genetic diversity. HPLC-DAD-HRMS analysis and subsequent database searching revealed that nine representative strains produced diverse bioactive compound profiles. These results detail the broad range of bioactive fimgi found in a shark＇s gills, revealing their biopharmaceutical potential. To the best of our knowledge, this is the first study characterizing shark gill fungi and their bioactivity.展开更多
AIM: To investigate the effects and mechanisms of Verapamil on cultured human colonic tumor (HCT) cells.METHODS: HCT cells were treated with different concentrations of Verapamil, and their proliferation was examined ...AIM: To investigate the effects and mechanisms of Verapamil on cultured human colonic tumor (HCT) cells.METHODS: HCT cells were treated with different concentrations of Verapamil, and their proliferation was examined by MTT assay. The areas of sub-diploid peak were measured by flow cytometry, and the DNA ladder was found by agarose gel electrophoresis. The characteristic changes in morphology were observed under light microscopy. The cell nuclei (propidium iodide labeled, PI-labeled) and cellular distribution and concentration of calcium (Fluo-3-labeled) were studied by using laser confocal scanning microscope.RESULTS: The proliferation of HCT cells was inhibited by different concentrations of Verapamil. With the increase in concentration of Verapamil, the percent of G0-G1 phase cells in HCT cells increased and that of S phase cells decreased. After treating with different concentrations of Verapamil, flow cytometry showed that HCT cells were enlarged in areas of sub-diploid in a dose-dependent manner. Gel electrophoresis results displayed a typical DNA ladder. On staining with Wrights-Giemsa, the typical cellular apoptosis morphologic changes were also observed. PI-labeled cell nuclei were found markedly changed. In addition, we inspected that the 100 μmol/L Verapamil could increase the intracellular calcium ion concentration [Ca2+]i in HCT cells.CONCLUSION: Verapamil can inhibit proliferation of HCT cells via inducing cell apoptosis.展开更多
Differential electrolytic potentiometry （DEP） was coupled with Flow injection analysis （FIA） technique for the determination of Procainamide in pharmaceutical preparations. Platinum electrodes were used as an indi...Differential electrolytic potentiometry （DEP） was coupled with Flow injection analysis （FIA） technique for the determination of Procainamide in pharmaceutical preparations. Platinum electrodes were used as an indicating system to follow the oxidation of Procainamide with cerium（IV）, and permanganate in an acidic medium. The oxidation reactions of Procainamide with Ce（IV） and/or permanganate are fast enough to permit its determination by flow injection in sulfuric acid media. The univariate method was employed to optimize the variables such as the current density, the flow rate, the oxidant concentration and the concentration of sulfuric acid. The proposed method was linear in the range 20-100 μg.mL^-1 , the DL and R2 values were 12 μg.mL^-1 and 0.995 respectively. The procedure was applied successfully to the determination of Procainamide in commercial tablets. The results of this study were favorably compared statistically with those obtained with official methods.展开更多
基金Supported by the National Natural Science Foundation of China(No.20902009)the National Science Foundation for Post-Doctoral Scientists of China(Nos.2011M500051,2012T50258)+2 种基金the Yang Fan Scarce Top Talent Project of Guangdong Province(to ZHANG Yi)the Program for Scientific Research Start-up Funds of Guangdong Ocean University(GDOU)(to ZHANG Yi)the Natural Science Research Project of GDOU(No.C14519)
文摘Until recently, little was known about the fungi found in shark gills and their biomedicinal potential. In this article, we described the isolation, bioactivity, diversity, and secondary metabolites of bioactive fungi from the gill of a shark （Carcharodon carcharias）. A total of 115 isolates were obtained and grown in 12 culture media. Fifty-eight of these isolates demonstrated significant activity in four antimicrobial, pesticidal, and cytotoxic bioassay models. Four randomly selected bioactive isolates inhibited human cancer cell proliferation during re-screening. These active isolates were segregated into 6 genera using the internal transcribed spacer-large subunit （ITS-LSU） rDNA-sequence BLAST comparison. Four genera, Penicillium, Aspergillus, Mucor, and Chaetomium were the dominant taxa. A phylogenic tree illustrated their intergenera and intragenera genetic diversity. HPLC-DAD-HRMS analysis and subsequent database searching revealed that nine representative strains produced diverse bioactive compound profiles. These results detail the broad range of bioactive fimgi found in a shark＇s gills, revealing their biopharmaceutical potential. To the best of our knowledge, this is the first study characterizing shark gill fungi and their bioactivity.
基金Supported by the Foundation of the National New Drug Research of China, No. 96-901-05-197
文摘AIM: To investigate the effects and mechanisms of Verapamil on cultured human colonic tumor (HCT) cells.METHODS: HCT cells were treated with different concentrations of Verapamil, and their proliferation was examined by MTT assay. The areas of sub-diploid peak were measured by flow cytometry, and the DNA ladder was found by agarose gel electrophoresis. The characteristic changes in morphology were observed under light microscopy. The cell nuclei (propidium iodide labeled, PI-labeled) and cellular distribution and concentration of calcium (Fluo-3-labeled) were studied by using laser confocal scanning microscope.RESULTS: The proliferation of HCT cells was inhibited by different concentrations of Verapamil. With the increase in concentration of Verapamil, the percent of G0-G1 phase cells in HCT cells increased and that of S phase cells decreased. After treating with different concentrations of Verapamil, flow cytometry showed that HCT cells were enlarged in areas of sub-diploid in a dose-dependent manner. Gel electrophoresis results displayed a typical DNA ladder. On staining with Wrights-Giemsa, the typical cellular apoptosis morphologic changes were also observed. PI-labeled cell nuclei were found markedly changed. In addition, we inspected that the 100 μmol/L Verapamil could increase the intracellular calcium ion concentration [Ca2+]i in HCT cells.CONCLUSION: Verapamil can inhibit proliferation of HCT cells via inducing cell apoptosis.
文摘Differential electrolytic potentiometry （DEP） was coupled with Flow injection analysis （FIA） technique for the determination of Procainamide in pharmaceutical preparations. Platinum electrodes were used as an indicating system to follow the oxidation of Procainamide with cerium（IV）, and permanganate in an acidic medium. The oxidation reactions of Procainamide with Ce（IV） and/or permanganate are fast enough to permit its determination by flow injection in sulfuric acid media. The univariate method was employed to optimize the variables such as the current density, the flow rate, the oxidant concentration and the concentration of sulfuric acid. The proposed method was linear in the range 20-100 μg.mL^-1 , the DL and R2 values were 12 μg.mL^-1 and 0.995 respectively. The procedure was applied successfully to the determination of Procainamide in commercial tablets. The results of this study were favorably compared statistically with those obtained with official methods.
